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1-Chloro-2-[(1Z)-3-Chloro-2-(4-Fluorophenyl)Prop-1-En-1-Yl]Benzene
Linshang Chemical
|
HS Code |
459910 |
| Chemical Formula | C15H10Cl2F |
| Molecular Weight | 279.147 g/mol |
| Physical State | Solid (usually) |
| Boiling Point | Estimated high boiling point due to molecular structure |
| Solubility In Water | Low solubility in water, likely hydrophobic |
| Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform |
| Appearance | Appearance likely colorless to pale - colored solid |
| Vapor Pressure | Low vapor pressure due to its non - volatile nature |
As an accredited 1-Chloro-2-[(1Z)-3-Chloro-2-(4-Fluorophenyl)Prop-1-En-1-Yl]Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 1 - chloro - 2 - [(1Z)-3 - chloro - 2 - (4 - fluorophenyl)prop - 1 - en - 1 - yl]benzene in sealed container. |
| Storage | 1 - chloro - 2 - [(1Z)-3 - chloro - 2 - (4 - fluorophenyl)prop - 1 - en - 1 - yl]benzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and oxidizing agents. Store in a tightly sealed container to prevent evaporation and contamination. Ensure the storage area is out of reach of children and unauthorized personnel. |
| Shipping | 1 - chloro - 2 - [(1Z)-3 - chloro - 2 - (4 - fluorophenyl)prop - 1 - en - 1 - yl]benzene is a chemical. Ship it in well - sealed, corrosion - resistant containers, following all hazardous chemical shipping regulations to ensure safe transit. |
Competitive 1-Chloro-2-[(1Z)-3-Chloro-2-(4-Fluorophenyl)Prop-1-En-1-Yl]Benzene prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615365006308 or mail to info@alchemist-chem.com.
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Tel: +8615365006308
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What is the chemical structure of 1-chloro-2- [ (1z) -3-chloro-2- (4-fluorophenyl) prop-1-en-1-yl] benzene
This is about the chemical structure of 1-chloro-2 - [ (1Z) -3-chloro-2 - (4-fluorophenyl) propane-1-ene-1-yl] benzene. According to its naming, "1-chloro-2 -" indicates that there is a chlorine atom at position 1 and a specific substituent at position 2 on the benzene ring. "[ ( 1Z) -3 -chloro-2 - (4 -fluorophenyl) propyl-1-enyl-1-yl] "part," (1Z) "indicates that the double bond configuration is Z-type, which means that the larger groups at both ends of the double bond are on the same side. 3-chlorine indicates that the 3 position of the propylene group has a chlorine atom, and the 2 - (4 -fluorophenyl) indicates that the 2 position of the propylene group is connected to the 4-fluorophenyl group. This compound has a phenyl ring as the core, and the 1 position of the chlorine atom of the phenyl ring is connected to a specific alkenyl substituent at the 2 position, and the alkenyl group has a chlorine atom and a fluor Its chemical structure is composed of benzene ring, chlorine atom, fluorine atom, carbon-carbon double bond and corresponding hydrocarbon group. Each atom and group are connected in an orderly manner according to the naming rules to build a unique chemical structure.
What are the physical properties of 1-chloro-2- [ (1z) -3-chloro-2- (4-fluorophenyl) prop-1-en-1-yl] benzene
1-Chloro-2- [ (1Z) -3-chloro-2- (4-fluorophenyl) propane-1-alkenyl] benzene, which is an organic compound. Looking at its structure, it can be seen that it is based on a benzene ring, and there are substituents containing chlorine, fluorophenyl and alkenyl groups connected to it.
In terms of its physical properties, it mostly exists in solid or liquid states at room temperature and pressure. Because it is an organic halide, containing chlorine and fluorine atoms, its relative molecular weight is high and the intermolecular force is strong, resulting in its melting point, boiling point or higher than that of the same series of non-halogenated compounds.
Its solubility, according to the principle of similar miscibility, should have good solubility in organic solvents such as dichloromethane, chloroform, toluene, etc. Because both organic solvents and the compound have organic properties, van der Waals forces can be formed between molecules, which is conducive to mutual solubility. However, in water, because of its large organic part and the absence of strong hydrophilic groups that can form hydrogen bonds with water, the solubility is very small.
The chromatic state of the compound, if there is no excessive extension of the conjugate system that causes it to absorb visible light and develop color, should usually be colorless or light yellow, which is the common chromatic state of most such halogenated aromatics. Its density is higher than that of water and common hydrocarbons due to chlorine and fluorine heavy atoms, or between 1.2 and 1.5 g/cm ³. The specific value varies with the exact structure and test conditions.
In summary, 1-chloro-2 - [ (1Z) -3-chloro-2 - (4-fluorophenyl) propyl-1-ene-1-yl] benzene has specific physical properties. In organic synthesis and related fields, its physical properties have an important impact on the selection of reaction conditions, product separation and purification.
In terms of its physical properties, it mostly exists in solid or liquid states at room temperature and pressure. Because it is an organic halide, containing chlorine and fluorine atoms, its relative molecular weight is high and the intermolecular force is strong, resulting in its melting point, boiling point or higher than that of the same series of non-halogenated compounds.
Its solubility, according to the principle of similar miscibility, should have good solubility in organic solvents such as dichloromethane, chloroform, toluene, etc. Because both organic solvents and the compound have organic properties, van der Waals forces can be formed between molecules, which is conducive to mutual solubility. However, in water, because of its large organic part and the absence of strong hydrophilic groups that can form hydrogen bonds with water, the solubility is very small.
The chromatic state of the compound, if there is no excessive extension of the conjugate system that causes it to absorb visible light and develop color, should usually be colorless or light yellow, which is the common chromatic state of most such halogenated aromatics. Its density is higher than that of water and common hydrocarbons due to chlorine and fluorine heavy atoms, or between 1.2 and 1.5 g/cm ³. The specific value varies with the exact structure and test conditions.
In summary, 1-chloro-2 - [ (1Z) -3-chloro-2 - (4-fluorophenyl) propyl-1-ene-1-yl] benzene has specific physical properties. In organic synthesis and related fields, its physical properties have an important impact on the selection of reaction conditions, product separation and purification.
What are the common uses of 1-chloro-2- [ (1z) -3-chloro-2- (4-fluorophenyl) prop-1-en-1-yl] benzene
1-Chloro-2- [ (1Z) -3-chloro-2- (4-fluorophenyl) propane-1-ene-1-yl] benzene, this is the scientific name of an organic compound. Its naming follows the systematic nomenclature to accurately describe the structure of the molecule.
In the field of chemical synthesis and other fields, this substance is often an important intermediate. Its common use is the first to promote drug development. Due to its specific chemical structure, drug molecules can be introduced through specific reaction paths to help regulate drug activity and improve pharmacokinetic properties. For example, in the development of some antidepressant drugs, it can be used as a key structural fragment to optimize the ability of drugs to bind to targets and enhance drug efficacy.
Furthermore, in the field of materials science, it also has potential applications. After modification, it may be used to prepare functional polymer materials, such as materials with special optical and electrical properties. Using it as a starting material through polymerization, it is expected to synthesize new conductive polymers for the manufacture of electronic devices.
In addition, in the preparation of fine chemicals, it can participate in many reactions to build complex molecular structures for the production of fragrances, additives, etc. For example, in the synthesis of high-end fragrances, its unique structure can endow fragrances with novel aroma characteristics.
Its common uses revolve around the fields of drugs, materials, and fine chemicals. By virtue of its structural characteristics, it provides key support for innovation and development in various fields.
In the field of chemical synthesis and other fields, this substance is often an important intermediate. Its common use is the first to promote drug development. Due to its specific chemical structure, drug molecules can be introduced through specific reaction paths to help regulate drug activity and improve pharmacokinetic properties. For example, in the development of some antidepressant drugs, it can be used as a key structural fragment to optimize the ability of drugs to bind to targets and enhance drug efficacy.
Furthermore, in the field of materials science, it also has potential applications. After modification, it may be used to prepare functional polymer materials, such as materials with special optical and electrical properties. Using it as a starting material through polymerization, it is expected to synthesize new conductive polymers for the manufacture of electronic devices.
In addition, in the preparation of fine chemicals, it can participate in many reactions to build complex molecular structures for the production of fragrances, additives, etc. For example, in the synthesis of high-end fragrances, its unique structure can endow fragrances with novel aroma characteristics.
Its common uses revolve around the fields of drugs, materials, and fine chemicals. By virtue of its structural characteristics, it provides key support for innovation and development in various fields.
What are the preparation methods of 1-chloro-2- [ (1z) -3-chloro-2- (4-fluorophenyl) prop-1-en-1-yl] benzene
1-Chloro-2- [ (1Z) -3-chloro-2- (4-fluorophenyl) propane-1-enyl-1-yl] benzene, the preparation method of this substance is often based on the path of chemical synthesis. One method can also be started by benzene derivatives containing corresponding substituents. First, take the raw material containing chlorophenyl ring and the allyl halide with fluorophenyl substitution, under appropriate reaction conditions, carry out nucleophilic substitution reaction. For example, a strong base is selected to take away the active hydrogen on the benzene ring, so that it forms a carboanion, and then interacts with the allyl halide to form a carbon-carbon bond.
Furthermore, it can be prepared by palladium-catalyzed cross-coupling reaction. The coupling reaction takes chlorophenylboronic acid and halogenated olefins with suitable substitutions as raw materials, and occurs in the presence of palladium catalyst, ligand and base. The reaction conditions are mild and the selectivity is good, and the carbon-carbon double bond structure of the target product can be accurately constructed.
Or use a step-by-step construction strategy. The unsaturated intermediate containing fluorophenyl is synthesized first, and then the subsequent reaction with chlorobenzene is carried out. For example, a derivative of 3-chloro-2 - (4-fluorophenyl) propane-1-ene-1-yl is first prepared, and it is connected to the 2-position of chlorobenzene through multiple reactions such as halogenation and nucleophilic substitution. Then the target compound 1-chloro-2 - [ (1Z) - 3-chloro-2 - (4-fluorophenyl) propane-1-ene-1-yl] benzene is obtained. Each method needs to consider the precise control of reaction conditions, the purity of raw materials and the cost in order to achieve the purpose of efficient preparation.
Furthermore, it can be prepared by palladium-catalyzed cross-coupling reaction. The coupling reaction takes chlorophenylboronic acid and halogenated olefins with suitable substitutions as raw materials, and occurs in the presence of palladium catalyst, ligand and base. The reaction conditions are mild and the selectivity is good, and the carbon-carbon double bond structure of the target product can be accurately constructed.
Or use a step-by-step construction strategy. The unsaturated intermediate containing fluorophenyl is synthesized first, and then the subsequent reaction with chlorobenzene is carried out. For example, a derivative of 3-chloro-2 - (4-fluorophenyl) propane-1-ene-1-yl is first prepared, and it is connected to the 2-position of chlorobenzene through multiple reactions such as halogenation and nucleophilic substitution. Then the target compound 1-chloro-2 - [ (1Z) - 3-chloro-2 - (4-fluorophenyl) propane-1-ene-1-yl] benzene is obtained. Each method needs to consider the precise control of reaction conditions, the purity of raw materials and the cost in order to achieve the purpose of efficient preparation.
What are the precautions for using 1-chloro-2- [ (1z) -3-chloro-2- (4-fluorophenyl) prop-1-en-1-yl] benzene?
1-Chloro-2 - [ (1Z) -3-chloro-2 - (4-fluorophenyl) propane-1-ene-1-yl] benzene, during use, all precautions should not be ignored.
Bear the brunt, this material is chemically active, and must be carefully protected when in contact. Appropriate protective equipment, such as gloves, goggles and protective clothing, is required to prevent it from coming into contact with the skin and eyes. If it is inadvertently touched, it may cause irritation or damage.
In addition, when it is stored, it is also necessary to pay attention. It should be placed in a cool, dry and well-ventilated place, away from fire and heat sources to prevent accidents. Because of its flammability, it may be dangerous in case of open flames and hot topics.
Where it is used, it must be well ventilated. The volatile gas of this substance may be harmful to human respiratory organs, and the circulating air can reduce its concentration in the air to protect people's health.
When operating, follow the regulations accurately, and do not do it arbitrarily. The steps of weighing and mixing should be rigorous to avoid improper operation and reaction deviation and prevent accidents.
In addition, after use, the remaining materials and waste need to be properly disposed of. Do not discard at will, should be in accordance with relevant laws and regulations, in the correct way to deal with the environment, free of pollution.
In short, the use of 1-chloro-2 - [ (1Z) -3 -chloro-2 - (4 -fluorophenyl) propane-1-ene-1-yl] benzene, when awe, pay attention to protection, storage, ventilation, operation and waste disposal to ensure safety.
Bear the brunt, this material is chemically active, and must be carefully protected when in contact. Appropriate protective equipment, such as gloves, goggles and protective clothing, is required to prevent it from coming into contact with the skin and eyes. If it is inadvertently touched, it may cause irritation or damage.
In addition, when it is stored, it is also necessary to pay attention. It should be placed in a cool, dry and well-ventilated place, away from fire and heat sources to prevent accidents. Because of its flammability, it may be dangerous in case of open flames and hot topics.
Where it is used, it must be well ventilated. The volatile gas of this substance may be harmful to human respiratory organs, and the circulating air can reduce its concentration in the air to protect people's health.
When operating, follow the regulations accurately, and do not do it arbitrarily. The steps of weighing and mixing should be rigorous to avoid improper operation and reaction deviation and prevent accidents.
In addition, after use, the remaining materials and waste need to be properly disposed of. Do not discard at will, should be in accordance with relevant laws and regulations, in the correct way to deal with the environment, free of pollution.
In short, the use of 1-chloro-2 - [ (1Z) -3 -chloro-2 - (4 -fluorophenyl) propane-1-ene-1-yl] benzene, when awe, pay attention to protection, storage, ventilation, operation and waste disposal to ensure safety.
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